Sham-Controlled RCT on 10kHz High-Frequency Spinal Cord Stimulation for Chronic Neuropathic Low Back Pain (Modulate-LBP)

Neuropathic Pain Clinical Trial

— Modulate-LBP  

Official title:

Multicentre, Double Blind, Randomised Sham-Controlled Trial of 10kHz High-Frequency Spinal Cord Stimulation for Chronic Neuropathic Low Back Pain (Modulate-LBP)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03470766
• Other study ID #: Modulate-LBP
• Status: Terminated
• Phase: N/A
• Start date: August 14, 2018
• Est. completion date: October 20, 2022

Study information

• Verified date: June 2024
• Source: Guy's and St Thomas' NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Multicentre, randomised, double-blinded, sham-controlled trial with parallel economic evaluation. Patients will be allocated 1:1 to activated 10kHz SCS plus usual care (intervention) or sham 10kHz SCS plus usual care (control) and followed up to 6 months.

Description:

The prevalence of chronic low back pain in the population is estimated to range between at 12% and 28% (1-4). Within this group an estimated 12-15% of adults suffer from chronic neuropathic lower back pain (CNLBP), have relatively greater pain severity, and account for more of the costs of this condition (5,6). This subgroup of people with CNLBP are the focus of the proposed trial.

The National Institute for Health and Care Excellence (NICE) recommends SCS for refractory neuropathic pain (TA159) (7). It is routinely used for people with predominant, neuropathic, radicular pain typically resulting from, or persisting after, spinal surgery (so-called failed back surgery syndrome (FBSS) (8-10). SCS has been shown to be cost effective for this indication (11).

Conventional SCS consists of the insertion of a medical wire (lead) introduced into the epidural space through a needle puncture. The lead is then positioned to target the pain by passing current into the lead from an external power source to generate a pins and needles sensation (paraesthesias) over the painful area. Analgesia occurs when the paraesthesia overlaps and therefore masks the painful area. Once pain reduction is demonstrated, the battery is implanted under the skin of the abdomen, flank or buttock. SCS is most commonly used in the treatment of leg pain of FBSS. However, due to lack of existing evidence and the difficulty of obtaining paraesthesia over the low back, SCS has traditionally not been recommended for treating patients with back pain without previous back surgery (10, 12).

High frequency 10kHz-SCS is a recent major advance in SCS technology. The current is delivered at 10kHz frequency as opposed to the 40 to 60Hz generated by the conventional SCS (13). The key advantages of a higher frequency current are:

10kHz-SCS has been shown to be superior (14) to conventional SCS in targeting residual low back pain following back surgery. Moreover, it does not generate any stimulation related sensations or paraesthesia so is preferred by patients as they are saved from needing to experience these distracting and occasional shocking sensations of conventional SCS. Therefore, 10kHz-SCS allows to smoothly conduct sham controlled or double blind studies in the field of SCS without the need for device modifications.

The lead applicant conducted an uncontrolled, multicentre, single arm study with 83 people with significant low back pain with or without leg pain, implanted with a 10kHz-SCS. At 24 months, the mean reported VAS score for back pain was 3.3 (SD 0.3), compared with 8.4 (SD 0.1) at baseline (pre-implant) and 2.7 (SD 0.3) at 6 months with 60% of subjects reporting >50% back pain relief. Similar improvements were observed in leg pain, disability, sleep and marked reductions in medication intake (15).

In a more recent multicentre RCT, 10kHz-SCS therapy demonstrated superiority to conventional low-frequency SCS in the treatment of post-surgical neuropathic pain. A total of 198 subjects with both back and leg pain were randomised in a 1:1 ratio to a 10 KHz-SCS or conventional SCS. 10kHz-SCS decreased back pain intensity by 67% compared to 44% in the conventional SCS arm (16). This decrease was sustained at 24 months (17).

The above mentioned studies focused on neuropathic back pain in the context of patients with previous spinal surgery. However, a small subset of patients without prior spine surgery that received 10kHz-SCS therapy in both these studies have shown good pain relief and functional improvements in both studies comparable to those with FBSS (14,16).

The investigators hypothesised that patients with CNLBP with no prior spine surgery would benefit from 10kHz-SCS. To evaluate this hypothesis, the investigators initially designed and conducted an open label uncontrolled pilot study in 21 patients with CNLBP and no prior spine surgery. 10kHz-SCS therapy significantly reduced back pain intensity by an average of 5.59 (SD 1.80) (-72.6% vs baseline) at 12 months in medically refractory low back pain patients with no past history of spine surgery. 90% of the implanted patients were classified as responders (i.e. VAS back pain reduction >50%) at 12 months. The investigators also observed a significant increase in physical function scores and health-related quality of life at one year post 10kHz-SCS implant. Mean pain intensity was reduced by 73% and disability measured by the Oswestry Disability Index was reduced by 48%. Opioid medication intake decreased by 64% and mean EQ-5D quality of life scores improved from 0.16 to 0.47. More importantly 75% of patients were able to return to employment(18). This improvement was sustained at 3 years follow up (19).

Following these promising results, the investigators now intend to undertake a fully powered RCT to confirm our hypothesis that 10kHz-SCS is beneficial for CNLBP patients with no prior back surgery.

To date 10kHz-SCS has not been formally tested against a sham control condition in order to isolate the therapeutic effects from those induced by placebo. It is very possible that some of the benefit reported may be due to a placebo effect (enhanced by a surgical procedure) or reporting bias in either the patient or assessor. The investigators have therefore specifically designed this fully powered double blind randomised sham controlled trial of 10kHz-SCS to address this major methodological limitation of previous studies.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 41
• Est. completion date: October 20, 2022
• Est. primary completion date: October 20, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Adults over the age of 18

2. Onset of low back pain > 12 months

3. Low back pain intensity > 60 out of 100mm on pain visual analogue scale (VAS)

4. Presence of clear component of neuropathic pain based on a PainDETECT Questionnaire score of >19 (we will monitor this inclusion criteria in the early stage of the trial and revise if necessary)

5. Degenerative disc disease confirmed by imaging or internal disc disruption as confirmed by discography

6. On stable pain medications, as determined by the Investigator, for at least 28 days prior to enrolling in this study and not change medication dosage without consulting Investigator

7. Legally able to provide informed consent

8. Able to comply with study-related requirements, procedures and visits

Exclusion Criteria:

1. Had previous spinal surgery

2. Chronic widespread pain

3. Subject has an active implanted device, whether turned on or off (e.g. pacemaker, intrathecal pump, deep brain stimulator etc.)

4. A current diagnosis of a progressive neurological disease such as multiple sclerosis, chronic inflammatory demyelinating polyneuropathy, rapidly progressive arachnoiditis, rapidly progressive diabetic peripheral neuropathy, brain or spinal cord tumour, or severe/critical central or foraminal spinal stenosis

5. Mechanical spine instability detected by a clinician (validation by flexion/extension films of lumbar spine within the past 6 months showing 4 mm or more translational movement or excessive angular movement manifested by >5 degrees segmental angular movement) e.g. any forms of spondylolisthesis

6. A medical condition or pain in other area(s), not intended to be treated with SCS, that could interfere with study procedures, accurate pain reporting, and/or confound evaluation of study endpoints, as determined by the Investigator

7. Bleeding diathesis such as coagulopathy or thrombocytopenia

8. Immunocompromised and at an increased risk for infection

9. Systemic infection or local infection that would contraindicate SCS placement

10. Metastatic malignant disease or active local malignant disease

11. Pregnant (if female and sexually active, subject must be using a reliable form of contraception, be surgically sterile or be at least 2 years post-menopausal)

12. Active alcohol, marijuana, recreational or prescription drug abuse or dependence or unwilling to stop/reduce excessive inappropriate medication.

13. Evidence of an active disruptive psychological or psychiatric disorder or other known condition significant enough to impact perception of pain, compliance of intervention and/or ability to evaluate treatment outcome as determined by the Investigator

14. Concomitant participation in another clinical trial (surgery, device or drug)

Related Conditions & MeSH terms

• Back Pain
• Chronic Low Back Pain
• Low Back Pain
• Neuralgia
• Neuropathic Pain
• Pain, Intractable
• Refractory Pain

Intervention

Device:
• Nevro Senza System (HF10 Therapy)
Nevro 10kHz High Frequency Spinal Cord Stimulation

Locations

Country	Name	City	State
United Kingdom	Guy's and St Thomas Hospital	London
United Kingdom	South Tees Hospitals NHS Foundation Trust	Middlesbrough

Sponsors (8)

Lead Sponsor	Collaborator
Guy's and St Thomas' NHS Foundation Trust	James Cook University Hospital, King's College London, National Institute for Health Research, United Kingdom, Pain And Neuromodulation Academic Research Centre (PANARC), University of Exeter, University of Liverpool, University of Oxford

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean VAS Back Pain (7 Day Subject VAS Pain Diary)	Changes in mean VAS back pain between intervention and control at 6 months post-randomisation	6 months post randomisation
Secondary	Oswestry disability index (v2.1a)	To compare disability between intervention and control at 1, 3, and 6 months post-randomisation.	1, 3, and 6 months post randomisation
Secondary	PHQ-9 Questionnaire	To compare depression between intervention and control at 1, 3, and 6 months post-randomisation.	1, 3, and 6 months post randomisation
Secondary	PSQI Questionnaire	To compare sleep quality between intervention and control at 1, 3, and 6 months post-randomisation.	1, 3, and 6 months post randomisation
Secondary	PGIC Questionnaire	To compare patients' global impression of change between intervention and control at 1, 3, and 6 months post-randomisation.	1, 3, and 6 months post randomisation
Secondary	EQ-5D Questionnaire	To compare health-related quality of life between intervention and control at 1, 3, and 6 months post-randomisation.	1, 3, and 6 months post randomisation
Secondary	Medication Usage	To compare medication usage between intervention and control at 1, 3, and 6 months post-randomisation.	1, 3, and 6 months post randomisation
Secondary	Sensation Map	To compare sensation maps between intervention and control at 1, 3, and 6 months post-randomisation.	1, 3, and 6 months post randomisation
Secondary	Healthcare utilisation, work status, work absence, and out of pocket expenses	To compare the cost-effectiveness of 10kHz-SCS between intervention and control at six months post-randomisation.	6 months post randomisation
Secondary	Safety/Adverse Events	To compare complications and adverse events at 6-months post-randomisation between intervention and control.	6 months post randomisation